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Bladder Urothelial Carcinoma in a Child: Case Report and Review of Literature
Marian Hanae Oda1, Danilo Vicente Dos Santos1, Adria Karina Farias2
1Medical School, Federal University of Parana, Curitiba, Brazil.
Insights
This case report details an 11-year-old boy diagnosed with bladder urothelial carcinoma (UC), a rare cancer in young individuals. The study highlights novel BRAF and KRAS gene mutations found in this pediatric UC case.
Area of Science:
- Urology
- Pediatric Oncology
- Genitourinary Pathology
Background:
- Bladder urothelial carcinoma (UC) is rare in pediatric populations, with limited data on risk factors and management protocols.
- UC typically affects older adults, making pediatric cases exceptional and requiring further investigation.
Observation:
- An 11-year-old boy presented with painful macroscopic hematuria, indicative of a bladder mass.
- Initial biopsy suggested urothelial papilloma, but a subsequent larger mass led to transurethral resection of the bladder (TURB).
Findings:
- Immunohistochemistry revealed low-grade papillary UC with a high-grade component, with tumor-free margins post-TURB.
- Genetic analysis identified previously undescribed BRAF and KRAS gene mutations in this pediatric UC case.
- The patient remains disease-free 2.5 years post-resection, indicating successful treatment.
Implications:
- This case adds valuable information to the understanding of rare pediatric bladder UC, particularly its genetic profile.
- The findings may inform future diagnostic and therapeutic strategies for young patients with UC.
- Highlights the importance of comprehensive genetic analysis in pediatric malignancies.
Abstract:
Bladder urothelial carcinoma (UC) it is the fifth most prevalent carcinoma in humans, nevertheless in children and young adults it's very rare. It usually occurs in older adults. Literature on UC in pediatric population is limited and important information (risk factors, follow-up protocols, etc.) are poorly defined. We present an 11-year-old boy with a painful macroscopic hematuria. Ultrasound revealed a heterogeneous intravesical mass without extravesical extension, which was confirmed by computed tomography (CT) and magnetic resonance imaging (MRI). The first biopsy was compatible with urothelial papilloma. After 1 year, he returned with a bigger mass. Transurethral resection of the bladder (TURB) was performed and immunohistochemistry showed low-grade papillary UC with a high-grade component, with tumor free margin. Tumor had mutations in the BRAF and KRAS genes. Two and a half years after the resection the patient has no recurrence. Less than 1% of bladder UC occur in the first two decades of life. Gross hematuria is a common symptom. Ultrasound is generally the first diagnostic tool. MRI is also helpful, but cystoscopy allows definitive diagnosis. Transurethral resection of the bladder (TURB) is the standard treatment, with good results and low recurrence rate, and it was the treatment of choice for our patient, that remains free of disease. The BRAF and KRAS gene mutations were never described before in pediatric UC. There are only few cases in literature of pediatric UC that present a tumor genetic profile; therefore, our case report adds more information to this very rare disease in children.
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